Enantioselective synthesis of β-aryl-γ-lactam derivatives via Heck–Matsuda desymmetrization of N-protected 2,5-dihydro-1H-pyrroles

Arnaldo G. de Oliveira Jr., Martí F. Wang, Rafaela C. Carmona, Danilo M. Lustosa, Sergei A. Gorbatov and Carlos R. D. Correia
Beilstein J. Org. Chem. 2024, 20, 940–949. https://doi.org/10.3762/bjoc.20.84

Supporting Information

Supporting Information File 1: Experimental procedures and characterization data for the new compounds.
Format: PDF Size: 9.8 MB Download

Cite the Following Article

Enantioselective synthesis of β-aryl-γ-lactam derivatives via Heck–Matsuda desymmetrization of N-protected 2,5-dihydro-1H-pyrroles
Arnaldo G. de Oliveira Jr., Martí F. Wang, Rafaela C. Carmona, Danilo M. Lustosa, Sergei A. Gorbatov and Carlos R. D. Correia
Beilstein J. Org. Chem. 2024, 20, 940–949. https://doi.org/10.3762/bjoc.20.84

How to Cite

de Oliveira, A. G., Jr..; Wang, M. F.; Carmona, R. C.; Lustosa, D. M.; Gorbatov, S. A.; Correia, C. R. D. Beilstein J. Org. Chem. 2024, 20, 940–949. doi:10.3762/bjoc.20.84

Download Citation

Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window below.
Citation data in RIS format can be imported by all major citation management software, including EndNote, ProCite, RefWorks, and Zotero.

Presentation Graphic

Picture with graphical abstract, title and authors for social media postings and presentations.
Format: PNG Size: 10.1 MB Download

Citations to This Article

Up to 20 of the most recent references are displayed here.

Scholarly Works

  • Chorro, T. H. D.; Kaussler, C.; Kolodiazhnaia, J. V.; Jensen, F.; Skrydstrup, T.; Correia, C. R. D. Tandem synthesis of enantioenriched spirolactones via one-pot Heck–Matsuda reactions directly from nitroarenes. Organic Chemistry Frontiers 2025. doi:10.1039/d4qo01979b
  • Burke, A. J.; Carreiro, E. P. 5th International Symposium on Synthesis and Catalysis (ISySyCat2023). Beilstein journal of organic chemistry 2024, 20, 2704–2707. doi:10.3762/bjoc.20.227
Other Beilstein-Institut Open Science Activities